ALS Group USA, Corp — FDA Facility Profile

FEI 2027219

ALS Group USA, Corp is an FDA-inspected facility (FEI 2027219) located in Torrance, CA, US. RegDataLab tracks 6 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Sep 4, 2026: Voluntary Action Indicated (VAI)
Inspections on record
6 (4 VAI, 2 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Sep 4, 2026Voluntary Action Indicated (VAI)Procedures not in writing, fully followed (21 CFR 211.22(d))
Investigations of discrepancies, failures (21 CFR 211.192)
Jun 5, 2023Voluntary Action Indicated (VAI)Equipment Design, Size and Location (21 CFR 211.63)
Feb 16, 2018Voluntary Action Indicated (VAI)Scientifically sound laboratory controls (21 CFR 211.160(b))
Jun 18, 2014No Action Indicated (NAI)No citations listed
Mar 1, 2012No Action Indicated (NAI)No citations listed
Jan 28, 2010Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
ALS Group USA, Corp
Location
Torrance, CA (US)
Source
inspections

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.